Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

LDQ 1980-02-01

CONPHAR SURGICAL RAZORR

Applicant Conphar, Inc.

K-Number K791798

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DQO 1980-02-01

DIAGNOSTIC INTRAVASCULAR CATHETER

Applicant Flomed, Inc.

K-Number K800171

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JRC 1980-02-01

MICROPITETTE

Applicant Meridian Diagnostics, Inc.

K-Number K792696

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DXN 1980-02-01

DINAMAP RESEARCH MONITOR 1245

Applicant Applied Medical Research

K-Number K800025

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GYE 1980-01-31

TELEMETRY SYSTEM XMT-1 & REC-1

Applicant Burdick Corp.

K-Number K792371

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DTC 1980-01-31

PACING SYSTEM ANALYZER PSA SCE-22

Applicant Ela Medical, Inc.

K-Number K791975

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DXY 1980-01-31

MICROTHIN-PI

Applicant Cardiac Pacemakers, Inc.

K-Number K800027

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JXG 1980-01-31

H-H FIFTH VENTRICLE

Applicant Holter-Hausner Intl.

K-Number K800168

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GWS 1980-01-31

MINI-CEARS COMPUTER (MODEL 1)

Applicant Bik Foundation, Inc.

K-Number K800001

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DTE 1980-01-31

CYNERGY MODEL 182

Applicant Cynergy

K-Number K792536

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DXY 1980-01-31

MICROTHIN-DI

Applicant Cardiac Pacemakers, Inc.

K-Number K800026

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GKL 1980-01-29

COULTER COUNTER-BLOOD CELL COUNTER

Applicant Coulter Electronics, Inc.

K-Number K792668

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